Dyna Flex, Intl. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dyna Flex, Intl. Physical Medicine ✕
4 devices
Cleared
Jan 23, 1991
ROMFLEX REHAB EQUIP EXTREMITIES UNIT
Physical Medicine
9d
Cleared
Jan 18, 1991
ROMFLEX REHAB EQUIP LATERAL FLEXION UNIT
Physical Medicine
4d
Cleared
Jan 18, 1991
ROMFLEX REHAB EQUIP CERVICAL FLEXOR UNIT
Physical Medicine
4d
Cleared
Dec 31, 1990
ROMFLEX REHABILITATION EQUIPMENT
Physical Medicine
33d